about
FOXP1 directly represses transcription of proapoptotic genes and cooperates with NF-κB to promote survival of human B cellsSystematic biases in DNA copy number originate from isolation proceduresDiabetes risk gene and Wnt effector Tcf7l2/TCF4 controls hepatic response to perinatal and adult metabolic demandE2F7 represses a network of oscillating cell cycle genes to control S-phase progressionAccurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.Identification of factors required for meristem function in Arabidopsis using a novel next generation sequencing fast forward genetics approach.Histological assessment of the effect of laser irradiation on skin wound healing in rats.Efficient double fragmentation ChIP-seq provides nucleotide resolution protein-DNA binding profiles.Identification of differential co-expressed gene networks in early rheumatoid arthritis achieving sustained drug-free remission after treatment with a tocilizumab-based or methotrexate-based strategy.Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing.Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitationsMajor and minor group rhinoviruses elicit differential signaling and cytokine responses as a function of receptor-mediated signal transduction.Interleukin-22 promotes intestinal-stem-cell-mediated epithelial regenerationNeonatal thymectomy reveals differentiation and plasticity within human naive T cellsE2f8 mediates tumor suppression in postnatal liver development.An siRNA screen for ATG protein depletion reveals the extent of the unconventional functions of the autophagy proteome in virus replication.Chemokines as possible targets in modulation of the secondary damage after acute spinal cord injury: a review.Genome-wide analysis reveals NRP1 as a direct HIF1α-E2F7 target in the regulation of motorneuron guidance in vivo.Primary colorectal cancers and their subsequent hepatic metastases are genetically different: implications for selection of patients for targeted treatment.Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization.Autoimmune disease-associated gene expression is reduced by BET-inhibitionWnt-induced transcriptional activation is exclusively mediated by TCF/LEF.FOXP3 can modulate TAL1 transcriptional activity through interaction with LMO2.The forkhead transcription factor FOXP1 represses human plasma cell differentiationFOXO3 selectively amplifies enhancer activity to establish target gene regulation.FOXP1 acts through a negative feedback loop to suppress FOXO-induced apoptosis.Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease.Genome-wide analysis of FOXO3 mediated transcription regulation through RNA polymerase II profiling.Adult stem cells in the small intestine are intrinsically programmed with their location-specific function.Integrated genome-wide analysis of transcription factor occupancy, RNA polymerase II binding and steady-state RNA levels identify differentially regulated functional gene classes.Gene expression profiling in human precision cut liver slices in response to the FXR agonist obeticholic acid.Extensive Association of Common Disease Variants with Regulatory Sequence.Inhibition of Super-Enhancer Activity in Autoinflammatory Site-Derived T Cells Reduces Disease-Associated Gene Expression.Tissue-specific mutation accumulation in human adult stem cells during life.A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genes.Enhancers reside in a unique epigenetic environment during early zebrafish development.Epidermal Growth Factor Receptor Expression Licenses Type-2 Helper T Cells to Function in a T Cell Receptor-Independent Fashion.Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples.Canonical Wnt signaling negatively modulates regulatory T cell function.The Atp1a1 gene from inbred Dahl salt sensitive rats does not contain the A1079T missense transversion.
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-5298-4852
@en
name
Michal Mokry
@ast
Michal Mokry
@en
Michal Mokry
@es
Michal Mokry
@nl
type
label
Michal Mokry
@ast
Michal Mokry
@en
Michal Mokry
@es
Michal Mokry
@nl
prefLabel
Michal Mokry
@ast
Michal Mokry
@en
Michal Mokry
@es
Michal Mokry
@nl
P106
P1153
8921358100
P21
P31
P496
0000-0002-5298-4852